Patient Perspective Midline Catheter in the Emergency Department

NCT ID: NCT05607238

Last Updated: 2023-06-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-31

Study Completion Date

2023-09-30

Brief Summary

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This study examines the patient satisfaction and perspective on the use of ultrasound guided midline intravenous catheters compared to standard ultrasound guided peripheral catheters.

Detailed Description

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Conditions

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Patient Satisfaction Patient Preference

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Ultrasound Guided Peripheral IV

Placement of 4-5cm angiocath under ultrasound guidance

Group Type ACTIVE_COMPARATOR

Ultrasound Guided Vascular Access - peripheral IV

Intervention Type PROCEDURE

Ultrasound guided vascular access with a peripheral IV catheter

Ultrasound Guided Midline Catheter

Placement of 10-15cm midline catheter under ultrasound guidance

Group Type EXPERIMENTAL

Ultrasound Guided Vascular Access - Midline catheter

Intervention Type PROCEDURE

Ultrasound guided vascular access with a midline IV catheter

Interventions

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Ultrasound Guided Vascular Access - Midline catheter

Ultrasound guided vascular access with a midline IV catheter

Intervention Type PROCEDURE

Ultrasound Guided Vascular Access - peripheral IV

Ultrasound guided vascular access with a peripheral IV catheter

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient in the emergency department
* Failed 2 or more conventional attempts at vascular access \*or\*
* history of requiring US guided vascular access
* US Fellowship trained physician available

Exclusion Criteria

* basilic vein access is contraindicated
* patient undergoing advanced resuscitation
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Wake Forest University Health Sciences

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Casey Glass, MD

Role: PRINCIPAL_INVESTIGATOR

Wake Forest University Health Sciences

Other Identifiers

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IRB00089914

Identifier Type: -

Identifier Source: org_study_id

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